Genetics of vestibular disorders: pathophysiological insights

Pathophysiology and treatment of motion sickness

(2015) John F. Golding et al.   CURRENT OPINION IN NEUROLOGY

Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis

(2015) Bethann S. Hromatka et al.   HUMAN MOLECULAR GENETICS

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

(2015) Zied Riahi et al.   PLoS One

Prevalence, Associated Factors, and Comorbid Conditions for Ménière’s Disease

(2014) Jessica S. Tyrrell et al.   EAR AND HEARING

A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine

(2014) Se-Kyung Oh et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5

(2014) Celia Zazo Seco et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Identification of Pathogenic Mechanisms ofCOCHMutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder

(2014) Seung-Hyun Bae et al.   HUMAN MUTATION

Dorsal root ganglionopathy is responsible for the sensory impairment in CANVAS

(2014) D. J. Szmulewicz et al.   NEUROLOGY

Intronic Variants in the NFKB1 Gene May Influence Hearing Forecast in Patients with Unilateral Sensorineural Hearing Loss in Meniere's Disease

(2014) Sonia Cabrera et al.   PLoS One

Familial clustering and genetic heterogeneity in Meniere's disease

(2013) T. Requena et al.   CLINICAL GENETICS

Genetics of dizziness

(2013) Teresa Requena et al.   CURRENT OPINION IN NEUROLOGY

Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere’s disease

(2013) Teresa Requena et al.   IMMUNOGENETICS

Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)

(2013) Qing Sang et al.   PLoS One

SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice

(2013) Xiangming Li et al.   PLoS Genetics

Meniere's disease might be an autoimmune condition?

(2012) A. Greco et al.   AUTOIMMUNITY REVIEWS

Autosomal recessive nonsyndromic deafness genes: a review

(2012) Duygu Duman   Frontiers in Bioscience-Landmark

A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies

(2012) Elina Hietikko et al.   INTERNATIONAL JOURNAL OF AUDIOLOGY

Future possibilities in migraine genetics

(2012) Laura Aviaja Rudkjobing et al.   JOURNAL OF HEADACHE AND PAIN

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

(2012) Jeong-In Baek et al.   Orphanet Journal of Rare Diseases

MICA-STR A.4 Is Associated With Slower Hearing Loss Progression in Patients With Ménière’s Disease

(2012) Irene Gazquez et al.   OTOLOGY & NEUROTOLOGY

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosis

(2011) David J. Szmulewicz et al.   Annals of the New York Academy of Sciences

Genetics of Recurrent Vertigo and Vestibular Disorders

(2011) Irene Gazquez et al.   CURRENT GENOMICS

Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28

(2011) Yanchao Han et al.   HUMAN MOLECULAR GENETICS

Genetic Aspects of Familial Ménière's Disease

(2011) Diana Arweiler-Harbeck et al.   OTOLOGY & NEUROTOLOGY

Molecular Analysis of Aquaporin Genes 1 to 4 in Patients with Menière’s Disease

(2010) Claudia Candreia et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct

(2010) Laurence Jonard et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

(2010) Yi Sun et al.   JOURNAL OF HUMAN GENETICS

Genetic Investigations of Meniere‘s Disease

(2010) Jeffrey T. Vrabec   OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

(2009) Colleen A. Campbell et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Vestibular Impairment in a Dutch DFNA15 Family with an L289F Mutation in POU4F3

(2009) F.J. Wendy van Drunen et al.   AUDIOLOGY AND NEURO-OTOLOGY

Capillary Endothelial Na+, K+, ATPase Transporter Homeostasis and a New Theory for Migraine Pathophysiology

(2009) Michael G. Harrington et al.   HEADACHE

Mutation Analysis of Slc26a4 in Mainland Chinese Patients with Enlarged Vestibular Aqueduct

(2009) Samuel Reyes et al.   OTOLARYNGOLOGY-HEAD AND NECK SURGERY

Familial Clustering of Migraine, Episodic Vertigo, and Ménière's Disease

(2009) Yoon-Hee Cha et al.   OTOLOGY & NEUROTOLOGY

A high-density association screen of 155 ion transport genes for involvement with common migraine

(2008) Dale R. Nyholt et al.   HUMAN MOLECULAR GENETICS

Familial Ménière's disease: clinical and genetic aspects

(2008) A W Morrison et al.   JOURNAL OF LARYNGOLOGY AND OTOLOGY

Gly460Trp α-Adducin Mutation as a Possible Mechanism Leading to Endolymphatic Hydrops in Ménière's Syndrome

(2008) Roberto Teggi et al.   OTOLOGY & NEUROTOLOGY